FDA UDI In Commercial Distribution 🇺🇸 United States

Bioseal Inc.

DI: 00630094180038 · Model: 18003/50 · BIOSEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bioseal Inc.
Primary DI
00630094180038
Version / Model
18003/50
Company Name
BIOSEAL
Labeler DUNS
186968939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-05
Public Version
1
Public Version Date
2023-10-13
Public Version Status
New
Public Device Record Key
3ece2676-58cb-4639-b66f-7a77651b617d

Device Description

Latex "0" RIngs for Ligators

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ECI BAND, ELASTIC, ORTHODONTIC

GMDN Terms

Code Name
38719 Polypectomy endoscopic ligator, single-use

Identifiers

Type ID
Package 10630094180035
Primary 00630094180038